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Title: 2,2'-Bipyridine  
Author: World Heritage Encyclopedia
Language: English
Subject: BPY, Proton-coupled electron transfer, Tris(bipyridine)ruthenium(II) chloride, Chelating agents, Redox indicator
Publisher: World Heritage Encyclopedia


Skeletal formula of 2,2'-bipyridine
Ball-and-stick model of the 2,2'-bipyridine molecule
IUPAC name
Other names
ChemSpider  Y
Jmol-3D images Image
RTECS number DW1750000
Molar mass 156.19 g·mol−1
Melting point 70 to 73 °C (158 to 163 °F; 343 to 346 K)
Boiling point 273 °C (523 °F; 546 K)
0 D
Main hazards toxic
R-phrases 25
S-phrases 36/37-45
Related compounds
Related compounds
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
 Y  (: Y/N?)

2,2'-Bipyridine (bipy or bpy (pronounced "bip-ee")) is an isomer of the bipyridine family. It is a bidentate chelating ligand, forming complexes with many transition metals. Ruthenium complex and platinum complexes of bipy exhibit intense luminescence, which may have practical applications.


  • Preparation and general properties 1
  • Coordination chemistry 2
    • Illustrative complexes 2.1
    • Tris-bipy complexes 2.2
  • References 3

Preparation and general properties

It is prepared by the dehydrogenation of pyridine using Raney nickel:[1]

2C5H5N → (C5H4N)2 + H2

Although uncoordinated bipyridine is often drawn with its nitrogen atoms in cis conformation, the lowest energy conformation both in solid state and in solution is in fact coplanar, with nitrogen atoms in trans position.[2] Protonated bipyridine adopts a cis conformation.[3] Upon binding to metal ions the related N,N-heterocyclic ligand phenanthroline does not incur an enthalpic and entropic penalty, and thus its complexes tend to be more stable.

Reflecting the popularity of this ligand design, many substituted variants of bipy have been described.[4][5]

Coordination chemistry

Illustrative complexes

Tris-bipy complexes

Bipyridine complexes absorb intensely in the visible part of the spectrum. The electronic transitions are attributed to metal-to-ligand charge transfer (MLCT). In the "tris(bipy) complexes" three bipyridine molecules coordinate to a metal ion, written as [M(bipy)3]n+ (M = metal ion; Cr, Fe, Co, Ru, Rh and so on; bipy = 2,2'-bipyridine). These complexes have six-coordinated, octahedral structures and two enantiomers as follows:

Three-dimensional view of the [Fe(bipy)3]2+ complex.

These and other homoleptic tris-2,2'-bipy complexes of many transition metals are electroactive. Often, both the metal centred and ligand centred electrochemical reactions are reversible one-electron reactions that can be observed by cyclic voltammetry. Under strongly reducing conditions, most tris(bipy) complexes can be reduced to neutral derivatives containing bipy ligands. Examples include M(bipy)3, where M = Al, Cr, Si.


  1. ^ Sasse, W. H. F. (1966). "2,2’-Bipyridine".  
  2. ^ Merritt, L. L.; Schroeder, E. (1956). "The Crystal Structure of 2,2'-Bipyridine". Acta Crystallographica 9 (10): 801–804.  
  3. ^ Göller, A.; Grummt, U.-W. (2000). "Torsional barriers in biphenyl, 2,2'-bipyridine and 2-phenylpyridine". Chemical Physics Letters 321 (5–6): 399–405.  
  4. ^ Smith, A. P.; Lamba, J. J. S.; Fraser, C. L. (2002). "Efficient Synthesis of Halomethyl-2,2'-Bipyridines: 4,4'-Bis(chloromethyl)-2,2'-Bipyridine".  
  5. ^ Smith, A. P.; Savage, S. A.; Love, J.; Fraser, C. L. (2002). "Synthesis of 4-, 5-, and 6-Methyl-2,2'-Bipyridine by a Negishi Cross-Coupling Strategy".  
  6. ^ Lay, P. A.; Sargeson, A. M.; Taube, H.; Chou, M. H.; Creutz, C. (1986). "Cis-Bis(2,2’-Bipyridine-N,N’) Complexes of Ruthenium(III)/(II) and Osmium(III)/(II)".  
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